UMR BIPAR, Ecole Nationale Vétérinaire d'Alfort, Anses, INRA, Université Paris-Est, Maisons-Alfort, France.
Unité Zoonoses Bactériennes, Anses, Université Paris-Est, Maisons-Alfort, France.
Parasit Vectors. 2018 Mar 9;11(1):163. doi: 10.1186/s13071-018-2661-7.
Anaplasma phagocytophilum is a zoonotic tick-borne intracellular alpha-proteobacterium causing tick-borne fever, which leads to significant economic losses in domestic ruminants in Europe. Its epidemiological cycles are complex and reservoir host species of bovine strains have not yet been identified. Given that little genetic information is available on strains circulating within a defined bovine environment, our objective was to assess the genetic diversity of A. phagocytophilum obtained from the same farms over time.
Blood samplings were performed several times in two European herds. In the French herd, 169 EDTA-blood samples were obtained from 115 cows (32 were sampled two to four times). In the German herd, 20 cows were sampled six times (120 EDTA-blood samples). The presence of A. phagocytophilum DNA was assessed using a qPCR targeting msp2. The positive DNA samples underwent MLST at nine genetic markers (typA, ctrA, msp4, pleD, recG, polA, groEL, gyrA, and ankA). For each locus, sequences were aligned with available bacterial sequences derived from cattle, horse, dog, and roe deer hosts, and concatenated neighbor joining trees were constructed using three to six loci.
Around 20% (57/289) of samples were positive. Forty positive samples from 23 French and six German cows (11 of them being positive at two time points) were sequenced. Six loci (typA, ctrA, msp4, pleD, recG, and polA) allowed to build concatenated phylogenetic trees, which led to two distinct groups of bovine variants in the French herd (hereafter called A and B), whereas only group A was detected in the German herd. In 42% of French samples, double chromatogram peaks were encountered in up to four loci. Eleven cows were found infected three weeks to 17 months after first sampling and harboured a new variant belonging to one or the other group.
Our results demonstrate the occurrence of two major bovine strain groups and the simultaneous infection of single cows by more than one A. phagocytophilum strain. This challenges the role of cattle as reservoirs for A. phagocytophilum. This role may be facilitated via long-term bacterial persistence in individual cows and active circulation at the herd scale.
嗜吞噬细胞无形体是一种由蜱传播的细胞内α-变形菌,可引起蜱传发热,在欧洲的家畜中造成重大经济损失。其流行病学循环复杂,牛株的储存宿主尚未确定。鉴于在特定牛环境中循环的菌株的遗传信息很少,我们的目标是随着时间的推移评估从同一农场获得的嗜吞噬细胞无形体的遗传多样性。
在两个欧洲牛群中多次进行血液采样。在法国牛群中,从 115 头奶牛中采集了 169 份 EDTA 血液样本(32 份样本采集了 2 到 4 次)。在德国牛群中,20 头奶牛被采集了 6 次(120 份 EDTA 血液样本)。使用靶向 msp2 的 qPCR 评估有无嗜吞噬细胞无形体 DNA。阳性 DNA 样本进行了 9 个遗传标记(typA、ctrA、msp4、pleD、recG、polA、groEL、gyrA 和 ankA)的 MLST。对于每个基因座,序列与源自牛、马、狗和狍宿主的细菌序列进行比对,并使用三个到六个基因座构建了邻接加入树。
约 20%(57/289)的样本呈阳性。23 头法国牛和 6 头德国牛的 40 份阳性样本(其中 11 份在两个时间点呈阳性)进行了测序。六个基因座(typA、ctrA、msp4、pleD、recG 和 polA)允许构建串联系统发育树,该树将法国牛群中的牛株分为两个不同的组(分别称为 A 和 B),而德国牛群中仅检测到组 A。在 42%的法国样本中,多达四个基因座中遇到了双峰色谱峰。在首次采样后 3 周到 17 个月,11 头奶牛被发现感染,并携带属于一个或另一个组的新变异株。
我们的结果表明存在两个主要的牛株群,以及单个牛的同时感染超过一种嗜吞噬细胞无形体株。这对牛作为嗜吞噬细胞无形体的储存宿主的作用提出了挑战。这种作用可能通过个体牛中的长期细菌持续存在和在牛群规模上的主动循环来促进。